Canonical Allele Identifier: CA1865515661

Gene: FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95249504_95249505delinsTG , CM000671.2:g.95249504_95249505delinsTG	GRCh38
NC_000009.11:g.98011786_98011787delinsTG , CM000671.1:g.98011786_98011787delinsTG	GRCh37
NC_000009.10:g.97051607_97051608delinsTG	NCBI36
NG_011707.1:g.73205_73206delinsCA , LRG_497:g.73205_73206delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.169-136_169-135delinsCA
ENST00000696262.1:c.-78-136_-78-135delinsCA	ENSP00000512510.1:n.-78-136_-78-135delinsCA
ENST00000696263.1:n.178-136_178-135delinsCA
ENST00000289081.8:c.-78-136_-78-135delinsCA MANE Select	ENSP00000289081.3:n.-78-136_-78-135delinsCA
ENST00000375305.6:c.-78-136_-78-135delinsCA	ENSP00000364454.1:n.-78-136_-78-135delinsCA
ENST00000490972.7:c.-78-136_-78-135delinsCA	ENSP00000479931.1:n.-78-136_-78-135delinsCA
ENST00000636777.1:n.20-175_20-174delinsCA
ENST00000647778.1:c.-78-136_-78-135delinsCA	ENSP00000498125.1:n.-78-136_-78-135delinsCA
ENST00000647882.1:c.-78-136_-78-135delinsCA	ENSP00000497025.1:n.-78-136_-78-135delinsCA
ENST00000648415.1:n.1561-136_1561-135delinsCA
ENST00000649519.1:c.-78-136_-78-135delinsCA	ENSP00000497630.1:n.-78-136_-78-135delinsCA
ENST00000649611.1:c.-78-136_-78-135delinsCA	ENSP00000497986.1:n.-78-136_-78-135delinsCA
ENST00000650176.1:n.103-136_103-135delinsCA
ENST00000289081.7:c.-78-136_-78-135delinsCA	ENSP00000289081.3:n.-78-136_-78-135delinsCA
ENST00000375305.5:c.-78-136_-78-135delinsCA	ENSP00000364454.1:n.-78-136_-78-135delinsCA
ENST00000433829.1:c.-78-136_-78-135delinsCA	ENSP00000406908.1:n.-78-136_-78-135delinsCA
ENST00000474949.1:n.185-136_185-135delinsCA
ENST00000490972.6:c.-78-136_-78-135delinsCA	ENSP00000479931.1:n.-78-136_-78-135delinsCA
NM_000136.2:c.-78-136_-78-135delinsCA , LRG_497t1:c.-78-136_-78-135delinsCA	NP_000127.2:n.-78-136_-78-135delinsCA
NM_001243743.1:c.-78-136_-78-135delinsCA	NP_001230672.1:n.-78-136_-78-135delinsCA
NM_001243744.1:c.-78-136_-78-135delinsCA	NP_001230673.1:n.-78-136_-78-135delinsCA
XM_006717001.1:c.-78-136_-78-135delinsCA	XP_006717064.1:n.-78-136_-78-135delinsCA
XM_006717002.2:c.-78-136_-78-135delinsCA	XP_006717065.1:n.-78-136_-78-135delinsCA
XM_006717004.2:c.-78-136_-78-135delinsCA	XP_006717067.1:n.-78-136_-78-135delinsCA
XM_011518365.1:c.-78-136_-78-135delinsCA	XP_011516667.1:n.-78-136_-78-135delinsCA
XM_011518366.1:c.-78-136_-78-135delinsCA	XP_011516668.1:n.-78-136_-78-135delinsCA
XM_011518367.1:c.-679-136_-679-135delinsCA	XP_011516669.1:n.-679-136_-679-135delinsCA
XM_006717001.3:c.-78-136_-78-135delinsCA	XP_006717064.1:n.-78-136_-78-135delinsCA
XM_006717002.4:c.-78-136_-78-135delinsCA	XP_006717065.1:n.-78-136_-78-135delinsCA
XM_006717004.4:c.-78-136_-78-135delinsCA	XP_006717067.1:n.-78-136_-78-135delinsCA
XM_011518365.3:c.-78-136_-78-135delinsCA	XP_011516667.1:n.-78-136_-78-135delinsCA
XM_011518366.3:c.-78-136_-78-135delinsCA	XP_011516668.1:n.-78-136_-78-135delinsCA
XM_011518367.2:c.-679-136_-679-135delinsCA	XP_011516669.1:n.-679-136_-679-135delinsCA
XM_017014452.2:c.-679-136_-679-135delinsCA	XP_016869941.1:n.-679-136_-679-135delinsCA
XM_017014453.1:c.-679-136_-679-135delinsCA	XP_016869942.1:n.-679-136_-679-135delinsCA
XM_017014454.1:c.-679-136_-679-135delinsCA	XP_016869943.1:n.-679-136_-679-135delinsCA
XM_024447451.1:c.-78-136_-78-135delinsCA	XP_024303219.1:n.-78-136_-78-135delinsCA
NM_000136.3:c.-78-136_-78-135delinsCA MANE Select	NP_000127.2:n.-78-136_-78-135delinsCA
NM_001243743.2:c.-78-136_-78-135delinsCA	NP_001230672.1:n.-78-136_-78-135delinsCA
NM_001243744.2:c.-78-136_-78-135delinsCA	NP_001230673.1:n.-78-136_-78-135delinsCA